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Structure of 1074-68-6
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2-(Methylthio)-4-pyrimidinecarboxaldehyde features a pyrimidine core functionalized with a methylthio group and an aldehyde moiety, enabling direct conjugation in synthetic transformations. This electron-deficient scaffold integrates readily into heterocyclic frameworks under mild conditions, offering high stability and compatibility with diverse reaction systems.
2-(Methylthio)-4-pyrimidinecarboxaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through standard aldehyde functionalization. Its methylthio group offers orthogonal reactivity for selective transformations, while the carboxaldehyde moiety facilitates condensation, coupling, and heterocyclization reactions. The compound exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: